Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000242507 Individual ID 00321290 Associated disease OI Phenotype details Osteogenesis imperfecta Type 1, subtype A (presence of dentinogenesis imperfecta), Diagnosis/Initial - Inheritance - Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Katarina Lindahl Database submission license No license selected Created by Katarina Lindahl Date created 2014-12-05 15:03:12 +01:00 (CET) Date last edited 2015-08-07 11:43:39 +02:00 (CEST)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.